SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2272308 | snp | C/T | 0.302686 | 0.244385 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163446 | GGCATCGGCAGTGGC[C/T]TGTCTCAGCTCTGTC | 102465519 |
rs2293432 | snp | A/C | 0.244205 | 0.249933 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164004 | ACGAGGACCTAGGTC[A/C]GGTGACAGGTGGATT | 102465519 |
rs12306627 | snp | C/T | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164382 | GGTGGGGTCTACCCT[C/T]GGCCGTGTAGATGAG | 102465519 |
rs35084322 | in-del | -/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163530 | GCCCAGCCTGGCCCT[-/G]GGGATGTCTACCTTG | 102465519 |
rs57142641 | snp | C/T | 0.00672897 | 0.0576125 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162989 | AGCCCCAGTTCCAAA[C/T]AGAGAAAGGCTAGTG | 102465519 |
rs61748839 | snp | C/T | 0.00692832 | 0.0584479 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163713 | GCTCCGGATGGCTGC[C/T]GCGTAGATGTCCTTG | 102465519 |
rs77746486 | snp | A/G | 0.00139218 | 0.0263467 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163563 | GAACTCGAGGTTGAT[A/G]TAGGGGAGGCCGCAG | 102465519 |
rs78121431 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164625 | CTAATTATGCTTGCT[C/T]TTTTTTTTTTTTGAG | 102465519 |
rs78614777 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164637 | GCTTTTTTTTTTTTT[G/T]GAGACGGAGTTTTGC | 102465519 |
rs78987995 | snp | A/G | 0.0444908 | 0.142359 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163794 | AGAGGCTGGGTCTGG[A/G]GGCCACACCCACTCA | 102465519 |
rs111277819 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163929 | TCTTAGTAAACCCCT[A/T]CTGCTGAGGACCCTC | 102465519 |
rs112704220 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164653 | GAGACGGAGTTTTGC[C/T]CTTGTTGCCCAGGCT | 102465519 |
rs114772167 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164031 | TCGTGTCATTGCCCA[G/T]GAACAGATGCTGCTG | 102465519 |
rs114947184 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163437 | TGTGGCAAGGACAGA[C/G]CTGAGACAGGCCACT | 102465519 |
rs140424049 | in-del | -/C | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164070 | GGCTGGCTGGCCGGG[-/C]CCAGCCCCTGCCAGC | 102465519 |
rs141828248 | snp | A/G | 0.000167434 | 0.00914817 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163629 | CAGCAGCTGCAGGGG[A/G]ATGATGGAGCCCAGG | 102465519 |
rs142106640 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164917 | GTGAGCCACTGCACC[C/T]AGACCGCTTTTTCTT | 102465519 |
rs145874584 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163372 | GGGGCAGGGTGCAAC[A/G]TGTGGGCTGTGAGCA | 102465519 |
rs147125643 | in-del | -/CCC | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163771 | AGGTGAGGGAGAACA[-/CCC]CCGCCGAAGAGGCTG | 102465519 |
rs147715633 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163799 | CTGGGTCTGGGGGCC[A/G]CACCCACTCAGCTGG | 102465519 |
rs149761829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163291 | AGGTCCAGGTGTCAG[A/G]AGCCCTGGAGCCCCA | 102465519 |
rs181634938 | snp | C/T | 0.000542446 | 0.0164599 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163651 | GAGCCCAGGCCGGCC[C/T]GCACGGCCGTCACGC | 102465519 |
rs182300912 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164747 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 102465519 |
rs183122979 | snp | A/T | | | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162788 | TTTTTTTTTTTAACC[A/T]TTTTTCTGCATTTAA | 102465519 |
rs183882784 | snp | C/T | 0.0133539 | 0.0806141 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163079 | GATCTTCATGGGGTA[C/T]GGGGGCACATGGGCA | 102465519 |
rs185247666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164766 | AGCTGGGATTACAGG[C/T]GCCCACCACCATGCC | 102465519 |
rs186770263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163802 | GGTCTGGGGGCCACA[C/T]CCACTCAGCTGGAGG | 102465519 |
rs188611917 | snp | A/G | 8.28837e-05 | 0.006437 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163208 | CTCCAGGGCCCCCCA[A/G]AAGAACTCGATGTGC | 102465519 |
rs189956579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164822 | AGACTGGGTTTCACT[A/G]TGTTGGCCAGGCTGG | 102465519 |
rs190623100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164692 | ATGGCGCAATCTTGG[C/G]TCGCTGCAACCCCTC | 102465519 |
rs192743323 | snp | C/T | | | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162768 | CCCAGCAAATTGTTT[C/T]TTTTTTTTTTTTTTT | 102465519 |
rs200268404 | snp | A/G | 0.000569285 | 0.0168617 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164214 | CTGTCAGGGCTCTCC[A/G]TGGCCAGGTGCTGGG | 102465519 |
rs201265123 | snp | C/G | 0.000844476 | 0.0205311 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163160 | GTTGCAGGCAAACTT[C/G]ATGAACTTGCACAGC | 102465519 |
rs202119425 | snp | C/T | 0.000657266 | 0.0181163 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164124 | GCCACAAGGATGTGC[C/T]GGCCCCGGCTGCACA | 102465519 |
rs367606627 | snp | C/T | 4.27451e-05 | 0.00462285 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163281 | TGGGGAGGAGAGGTC[C/T]AGGTGTCAGGAGCCC | 102465519 |
rs368281795 | snp | A/G | 0.000132514 | 0.00813876 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163151 | GCGCTCCTGGTTGCA[A/G]GCAAACTTGATGAAC | 102465519 |
rs369547696 | snp | G/T | 1.75145e-05 | 0.00295921 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164153 | CAGCTCCACCTCCTC[G/T]CCCGTCATGGTCAGG | 102465519 |
rs369564664 | snp | C/T | 0.00112945 | 0.0237371 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164096 | CCAGCCCCTGACACG[C/T]GCACACACTCACGCC | 102465519 |
rs370063916 | snp | A/C/T | 3.34965e-05 | 0.00409235 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164242 | GGGAGGCGATCTCAG[A/C/T]GCACAGGGCCTCCAG | 102465519 |
rs371033442 | snp | A/G | 0.000156924 | 0.0088565 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164321 | ATGAGGCCATGGGAG[A/G]TGGAACCCTGATCCC | 102465519 |
rs371115604 | snp | C/T | 8.36897e-05 | 0.00646822 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164233 | CCAGGTGCTGGGAGG[C/T]GATCTCAGCGCACAG | 102465519 |
rs371332898 | snp | C/G | 0.000163987 | 0.00905353 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163294 | TCCAGGTGTCAGGAG[C/G]CCTGGAGCCCCACCT | 102465519 |
rs371389017 | snp | C/G | 3.31697e-05 | 0.00407231 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163106 | GGCAGTGTCGGGACC[C/G]CCATCTTTGCAGGGG | 102465519 |
rs371880099 | snp | C/G | 8.28246e-05 | 0.00643471 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163172 | CTTGATGAACTTGCA[C/G]AGCTCCTCCTGGGTG | 102465519 |
rs372003631 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163925 | GTTTTCTTAGTAAAC[C/T]CCTTCTGCTGAGGAC | 102465519 |
rs372573928 | snp | C/T | 0.000190221 | 0.0097506 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164156 | CTCCACCTCCTCGCC[C/T]GTCATGGTCAGGTAG | 102465519 |
rs374029714 | snp | C/T | 3.31724e-05 | 0.00407248 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163216 | CCCCCCAGAAGAACT[C/T]GATGTGCTGGTCCGT | 102465519 |
rs374497789 | snp | C/T | 0.000461969 | 0.0151911 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164295 | AGGGTGGAGGCAGAG[C/T]GAGGCTCATTATGAG | 102465519 |
rs375061280 | snp | A/T | 0.000161987 | 0.00899817 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164091 | CCCTGCCAGCCCCTG[A/T]CACGCGCACACACTC | 102465519 |
rs375330854 | snp | C/T | 0.000326371 | 0.0127702 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164130 | AGGATGTGCCGGCCC[C/T]GGCTGCACAGCTCCA | 102465519 |
rs375445453 | snp | A/G | 3.70501e-05 | 0.00430391 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163017 | GTGTGTCCCTACTTG[A/G]GACATGGCCAGGGGA | 102465519 |
rs375590063 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163976 | ATCCTGCCTCATCTC[C/T]CTCTCCTGGTGAAAT | 102465519 |
rs375635285 | snp | C/T | 1.65839e-05 | 0.00287953 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163107 | GCAGTGTCGGGACCC[C/T]CATCTTTGCAGGGGC | 102465519 |
rs375938583 | snp | C/T | 0.000187982 | 0.00969308 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163551 | GTCTACCTTGAGGAA[C/T]TCGAGGTTGATGTAG | 102465519 |
rs376711869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164922 | CCACTGCACCCAGAC[C/T]GCTTTTTCTTTTTTT | 102465519 |
rs377053677 | snp | A/G | 0.000938702 | 0.0216442 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163656 | CAGGCCGGCCCGCAC[A/G]GCCGTCACGCACTCC | 102465519 |
rs377506093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162895 | TGGCTGGTTCCTGCC[A/G]GGCCCTAATCCTCAA | 102465519 |
rs527298215 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164642 | TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTTG | 102465519 |
rs527424635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165265 | CAGAGGCCTGAGACC[A/G]ATACCAGATGATACT | 102465519 |
rs527546674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164015 | CACCTGACCTAGGTC[C/T]TCGTGTCATTGCCCA | 102465519 |
rs528812083 | snp | C/G | 0.000182208 | 0.00954311 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163184 | GCACAGCTCCTCCTG[C/G]GTGAACATCTCCAGG | 102465519 |
rs528961462 | snp | A/G | | | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162929 | TGTCTGAGTTTTGGC[A/G]CGTGGGGCTCCTGTT | 102465519 |
rs529747953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164886 | CTCAGCCTTCCAAAG[C/T]GCTGGGATTACAGGT | 102465519 |
rs532706721 | in-del | -/GCCAGCCCCT | 0.00183206 | 0.0302105 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164069 | TGGCTGGCTGGCCGG[-/GCCAGCCCCT]GCCAGCCCCTGCCAG | 102465519 |
rs533056922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164446 | CATCAGTTCAGGGCC[A/G]GGCGTGTGACCCAGG | 102465519 |
rs533087892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163855 | GGCCTGGGGCCCAGC[C/T]GCCCTGGTCATCCCA | 102465519 |
rs533769191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162837 | CATTCTGGATTTTCA[A/G]CTTCTTTTAAGATAT | 102465519 |
rs534136597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163512 | TGGGGCTCACCACCT[C/G]CCCGCCCAGCCTGGC | 102465519 |
rs535516940 | snp | A/G | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163612 | AGTGGGCTGAGCATG[A/G]TCAGCAGCTGCAGGG | 102465519 |
rs535743680 | snp | A/C | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164351 | CCAGGTGGCTGGGTA[A/C]ACCCCAAGCGCAGCT | 102465519 |
rs537674422 | snp | C/T | 0.00782583 | 0.0620618 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164067 | CCCTGGCTGGCTGGC[C/T]GGGCCAGCCCCTGCC | 102465519 |
rs540965990 | snp | C/G | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163719 | GATGGCTGCCGCGTA[C/G]ATGTCCTTGTTCTCC | 102465519 |
rs542012726 | snp | G/T | 0.000326554 | 0.0127738 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163270 | TGGTGTGGGCCTGGG[G/T]AGGAGAGGTCCAGGT | 102465519 |
rs542595027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165308 | GGATTTGGCCCTGCC[G/T]GAAGTCAAACCCATC | 102465519 |
rs544745123 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165154 | TTGAACTCCTGACCT[C/T]GTGATCTACCCGCCT | 102465519 |
rs544961944 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165069 | GGGATTACAGGCACC[C/T]GCCACCATGCCTGGC | 102465519 |
rs545092155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164540 | CTCACTGGCATGGAC[C/T]GACTATGATGGGAAA | 102465519 |
rs545772641 | snp | C/T | 0.000767361 | 0.0195727 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163687 | ACATTCTGCAGCTCC[C/T]GCAGCCGCAGGCTCC | 102465519 |
rs545807973 | snp | C/T | | | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162930 | GTCTGAGTTTTGGCA[C/T]GTGGGGCTCCTGTTC | 102465519 |
rs547440179 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163856 | GCCTGGGGCCCAGCC[A/G]CCCTGGTCATCCCAG | 102465519 |
rs548543216 | in-del | -/TGAT | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164329 | TGGGAGGTGGAACCC[-/TGAT]TGATCCCCAGGTGGC | 102465519 |
rs549270232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164029 | CCTCGTGTCATTGCC[C/G]AGGAACAGATGCTGC | 102465519 |
rs549747227 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164018 | CTGACCTAGGTCCTC[A/G]TGTCATTGCCCAGGA | 102465519 |
rs550697417 | snp | A/G | 0.000394878 | 0.0140457 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163298 | GGTGTCAGGAGCCCT[A/G]GAGCCCCACCTACCC | 102465519 |
rs553952531 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165029 | TGGGTTCAAGCAATT[C/T]TCTGCCTCAGGCTCC | 102465519 |
rs555564729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162894 | ATGGCTGGTTCCTGC[C/T]GGGCCCTAATCCTCA | 102465519 |
rs555824604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164980 | CAGCTGGAGTGCAGT[A/G]GCGCAATCTCAGCTC | 102465519 |
rs555940034 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164541 | TCACTGGCATGGACC[A/G]ACTATGATGGGAAAC | 102465519 |
rs555971026 | snp | C/T | 0.000432121 | 0.0146926 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164094 | TGCCAGCCCCTGACA[C/T]GCGCACACACTCACG | 102465519 |
rs556039865 | snp | A/G | 0 | 0 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164240 | CTGGGAGGCGATCTC[A/G]GCGCACAGGGCCTCC | 102465519 |
rs556748614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165070 | GGATTACAGGCACCC[A/G]CCACCATGCCTGGCT | 102465519 |
rs557862489 | snp | A/G | 2.20524e-05 | 0.0033205 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164131 | GGATGTGCCGGCCCC[A/G]GCTGCACAGCTCCAC | 102465519 |
rs558239335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164897 | AAAGCGCTGGGATTA[C/T]AGGTGTGAGCCACTG | 102465519 |
rs559854710 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164600 | GTGCGCTGGGAGAGA[A/C]TGCTTGAGGCTAATT | 102465519 |
rs560216408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165165 | ACCTCGTGATCTACC[C/T]GCCTCAGCCTCCCAA | 102465519 |
rs560687679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164383 | GTGGGGTCTACCCTC[A/G]GCCGTGTAGATGAGC | 102465519 |
rs562592155 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163853 | GAGGCCTGGGGCCCA[A/G]CCGCCCTGGTCATCC | 102465519 |
rs563109255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164384 | TGGGGTCTACCCTCG[G/T]CCGTGTAGATGAGCA | 102465519 |
rs563297363 | snp | C/T | 1.88525e-05 | 0.00307016 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162999 | CCAAACAGAGAAAGG[C/T]TAGTGTGTCCCTACT | 102465519 |
rs564542020 | snp | C/T | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163702 | CGCAGCCGCAGGCTC[C/T]GGATGGCTGCCGCGT | 102465519 |
rs564650307 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163091 | GTACGGGGGCACATG[A/G]GCAGTGTCGGGACCC | 102465519 |
rs566632838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163455 | GAGACAGGCCACTGC[C/T]GATGCCTGCTGCTGG | 102465519 |
rs567203853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164694 | GGCGCAATCTTGGCT[C/T]GCTGCAACCCCTCGC | 102465519 |
rs572503467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164707 | CTCGCTGCAACCCCT[A/C]GCCTCCTGGGTGCAA | 102465519 |
rs572957691 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162772 | GCAAATTGTTTCTTT[C/T]TTTTTTTTTTTAACC | 102465519 |
rs573784336 | snp | A/G | 0.000520291 | 0.0161206 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163575 | GATGTAGGGGAGGCC[A/G]CAGGTGCGCAGCTCC | 102465519 |
rs574370839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165024 | CCTCCTGGGTTCAAG[A/C]AATTCTCTGCCTCAG | 102465519 |
rs575248985 | snp | A/G | 0.000161251 | 0.00897773 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163037 | TGGCCAGGGGAGGGC[A/G]GTACCTGCTGTGCCA | 102465519 |
rs576999187 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165178 | CCCGCCTCAGCCTCC[C/G]AAAGTGCTGGGATTA | 102465519 |
rs578224279 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165112 | TTTTAGTAGAGACGG[A/C/G]GTTTCACCACCTTGG | 102465519 |
rs745626274 | snp | A/G | 0.000466364 | 0.0152632 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164097 | CAGCCCCTGACACGC[A/G]CACACACTCACGCCA | 102465519 |
rs745976753 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164516 | TCTGTTTGGAGGCAG[C/T]GATCCTCTCTCACTG | 102465519 |
rs746492036 | in-del | -/G | 1.73791e-05 | 0.00294775 | frameshift-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163056 | CCTGCTGTGCCATCT[-/G]GGGGGGCGATCTTCA | 102465519 |
rs746911962 | snp | C/T | 3.37558e-05 | 0.00410814 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164121 | CACGCCACAAGGATG[C/T]GCCGGCCCCGGCTGC | 102465519 |
rs747501111 | snp | C/G | 1.65658e-05 | 0.00287795 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163183 | TGCACAGCTCCTCCT[C/G]GGTGAACATCTCCAG | 102465519 |
rs747556052 | snp | G/T | 1.71891e-05 | 0.00293159 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163058 | TGCTGTGCCATCTGG[G/T]GGGGCGATCTTCATG | 102465519 |
rs748198079 | snp | C/T | 3.05497e-05 | 0.00390819 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163302 | TCAGGAGCCCTGGAG[C/T]CCCACCTACCCAGTG | 102465519 |
rs748251023 | snp | A/G | 1.65666e-05 | 0.00287802 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163191 | TCCTCCTGGGTGAAC[A/G]TCTCCAGGGCCCCCC | 102465519 |
rs748268619 | in-del | -/AGAGGGT | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163925 | TTTTCTTAGTAAACC[-/AGAGGGT]CCTTCTGCTGAGGAC | 102465519 |
rs749457917 | snp | A/G | 1.71852e-05 | 0.00293127 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163358 | CCAGGCCCAATCCTG[A/G]GGCAGGGTGCAACGT | 102465519 |
rs750249148 | snp | C/T | 7.44477e-05 | 0.00610068 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163013 | GCTAGTGTGTCCCTA[C/T]TTGGGACATGGCCAG | 102465519 |
rs750502782 | snp | A/T | 1.71917e-05 | 0.00293182 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164303 | GGCAGAGCGAGGCTC[A/T]TTATGAGGCCATGGG | 102465519 |
rs750625494 | snp | C/T | 1.67528e-05 | 0.00289415 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164213 | GCTGTCAGGGCTCTC[C/T]GTGGCCAGGTGCTGG | 102465519 |
rs750754319 | snp | C/G | 1.65649e-05 | 0.00287788 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163166 | GGCAAACTTGATGAA[C/G]TTGCACAGCTCCTCC | 102465519 |
rs751030696 | snp | C/G | 1.85475e-05 | 0.00304523 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163016 | AGTGTGTCCCTACTT[C/G]GGACATGGCCAGGGG | 102465519 |
rs751467667 | snp | G/T | 6.6335e-05 | 0.00575874 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163126 | CTTTGCAGGGGCAGG[G/T]GAACGGGATGCGCTC | 102465519 |
rs751973866 | snp | A/G | 6.65196e-05 | 0.00576675 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163284 | GGAGGAGAGGTCCAG[A/G]TGTCAGGAGCCCTGG | 102465519 |
rs752271888 | snp | A/T | 1.65655e-05 | 0.00287793 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163143 | AACGGGATGCGCTCC[A/T]GGTTGCAGGCAAACT | 102465519 |
rs752326847 | snp | C/T | 7.31984e-05 | 0.00604928 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163026 | TACTTGGGACATGGC[C/T]AGGGGAGGGCGGTAC | 102465519 |
rs753121234 | snp | C/T | 0.000176538 | 0.0093935 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163773 | GGTGAGGGAGAACAC[C/T]GCCGAAGAGGCTGGG | 102465519 |
rs753815884 | snp | A/C | 1.68977e-05 | 0.00290665 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164176 | TGGTCAGGTAGGTGA[A/C]CCTGCAGCAGGGCTT | 102465519 |
rs755482629 | snp | C/T | 2.74473e-05 | 0.00370444 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163296 | CAGGTGTCAGGAGCC[C/T]TGGAGCCCCACCTAC | 102465519 |
rs755661535 | snp | C/T | | | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163655 | CCAGGCCGGCCCGCA[C/T]GGCCGTCACGCACTC | 102465519 |
rs755824170 | snp | C/G | 1.80755e-05 | 0.00300623 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163033 | GACATGGCCAGGGGA[C/G]GGCGGTACCTGCTGT | 102465519 |
rs756114700 | snp | C/T | 3.27209e-05 | 0.00404467 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163309 | CCCTGGAGCCCCACC[C/T]ACCCAGTGCCTCCCC | 102465519 |
rs756987830 | snp | G/T | 1.84851e-05 | 0.0030401 | intron-variant, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163272 | GTGTGGGCCTGGGGA[G/T]GAGAGGTCCAGGTGT | 102465519 |
rs757360916 | snp | C/T | 1.68823e-05 | 0.00290532 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164178 | GTCAGGTAGGTGAAC[C/T]TGCAGCAGGGCTTGT | 102465519 |
rs758133588 | snp | C/T | | | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163715 | TCCGGATGGCTGCCG[C/T]GTAGATGTCCTTGTT | 102465519 |
rs758555503 | snp | A/G | 1.73782e-05 | 0.00294767 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164317 | CATTATGAGGCCATG[A/G]GAGGTGGAACCCTGA | 102465519 |
rs759466323 | snp | A/G | 3.31752e-05 | 0.00407265 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163217 | CCCCCAGAAGAACTC[A/G]ATGTGCTGGTCCGTC | 102465519 |
rs759519228 | snp | C/T | 1.65699e-05 | 0.00287831 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163130 | GCAGGGGCAGGTGAA[C/T]GGGATGCGCTCCTGG | 102465519 |
rs760008766 | snp | A/G | 7.21059e-05 | 0.00600398 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163716 | CCGGATGGCTGCCGC[A/G]TAGATGTCCTTGTTC | 102465519 |
rs760024312 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163383 | CAACGTGTGGGCTGT[A/G]AGCACAGGGAGATGA | 102465519 |
rs760129905 | snp | A/G | 3.40599e-05 | 0.0041266 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163256 | CCCCACTTGGTACAT[A/G]GTGTGGGCCTGGGGA | 102465519 |
rs760853136 | snp | A/C | 1.92062e-05 | 0.00309883 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162968 | TCCCTTCACATGGGG[A/C]CTGGCAGCCCCAGTT | 102465519 |
rs760968860 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163641 | GGGGATGATGGAGCC[C/T]AGGCCGGCCCGCACG | 102465519 |
rs761022667 | snp | C/G | 3.48481e-05 | 0.00417406 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164154 | AGCTCCACCTCCTCG[C/G]CCGTCATGGTCAGGT | 102465519 |
rs761126386 | snp | A/G | 1.69729e-05 | 0.0029131 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164282 | ATCATTGATCTGGAG[A/G]GTGGAGGCAGAGCGA | 102465519 |
rs761302717 | snp | A/T | 0.000203853 | 0.0100938 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163669 | ACGGCCGTCACGCAC[A/T]CCACATTCTGCAGCT | 102465519 |
rs761406553 | snp | A/G | 0.000193678 | 0.00983877 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164125 | CCACAAGGATGTGCC[A/G]GCCCCGGCTGCACAG | 102465519 |
rs761661183 | in-del | -/C | 3.44828e-05 | 0.00415213 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164085 | GCCAGCCCCTGCCAG[-/C]CCCTGACACGCGCAC | 102465519 |
rs761789572 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164887 | TCAGCCTTCCAAAGC[A/G]CTGGGATTACAGGTG | 102465519 |
rs762118867 | snp | A/G | 1.65982e-05 | 0.00288077 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163100 | CACATGGGCAGTGTC[A/G]GGACCCCCATCTTTG | 102465519 |
rs762360924 | snp | A/G | 1.71138e-05 | 0.00292516 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164296 | GGGTGGAGGCAGAGC[A/G]AGGCTCATTATGAGG | 102465519 |
rs762645048 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164588 | CCACCTCTGCCCGTG[C/T]GCTGGGAGAGACTGC | 102465519 |
rs762690524 | snp | C/G | 1.67767e-05 | 0.00289622 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164250 | ATCTCAGCGCACAGG[C/G]CCTCCAGCTCGGTCT | 102465519 |
rs762880130 | snp | C/T | 5.57553e-05 | 0.00527964 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163014 | CTAGTGTGTCCCTAC[C/T]TGGGACATGGCCAGG | 102465519 |
rs763197098 | in-del | -/G | 1.73564e-05 | 0.00294583 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164316 | TCATTATGAGGCCAT[-/G]GGAGGTGGAACCCTG | 102465519 |
rs763630508 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164931 | CCAGACCGCTTTTTC[-/T]TTTTTTTTTTTTTGA | 102465519 |
rs763766190 | snp | A/G | 6.98348e-05 | 0.00590868 | missense, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163263 | TGGTACATGGTGTGG[A/G]CCTGGGGAGGAGAGG | 102465519 |
rs764178730 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164717 | CCCCTCGCCTCCTGG[A/G]TGCAAGCAATTATCC | 102465519 |
rs764471814 | snp | A/G | 1.70568e-05 | 0.0029203 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164286 | TTGATCTGGAGGGTG[A/G]AGGCAGAGCGAGGCT | 102465519 |
rs765293011 | snp | G/T | 6.86024e-05 | 0.00585632 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164299 | TGGAGGCAGAGCGAG[G/T]CTCATTATGAGGCCA | 102465519 |
rs766239246 | snp | A/T | 1.85675e-05 | 0.00304687 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163015 | TAGTGTGTCCCTACT[A/T]GGGACATGGCCAGGG | 102465519 |
rs766299664 | snp | A/G | 1.65718e-05 | 0.00287848 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163125 | TCTTTGCAGGGGCAG[A/G]TGAACGGGATGCGCT | 102465519 |
rs766643313 | snp | A/G | 1.74051e-05 | 0.00294996 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164320 | TATGAGGCCATGGGA[A/G]GTGGAACCCTGATCC | 102465519 |
rs767002103 | snp | A/G | 1.65671e-05 | 0.00287807 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163138 | AGGTGAACGGGATGC[A/G]CTCCTGGTTGCAGGC | 102465519 |
rs767145513 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165093 | CCTGGCTAATTTTTG[-/T]TATTTTTAGTAGAGA | 102465519 |
rs767449680 | snp | C/T | 6.65347e-05 | 0.0057674 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163229 | CTCGATGTGCTGGTC[C/T]GTCTCCATCAGCCCC | 102465519 |
rs767981814 | snp | C/T | 1.92888e-05 | 0.00310549 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164138 | CCGGCCCCGGCTGCA[C/T]AGCTCCACCTCCTCG | 102465519 |
rs768426467 | snp | A/G | 1.67351e-05 | 0.00289263 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164234 | CAGGTGCTGGGAGGC[A/G]ATCTCAGCGCACAGG | 102465519 |
rs768520663 | in-del | -/GCCGGGCCAGCCCCTGCCAGCCCCT | 3.73462e-05 | 0.00432108 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164065 | TACCCTGGCTGGCTG[-/GCCGGGCCAGCCCCTGCCAGCCCCT]GACACGCGCACACAC | 102465519 |
rs768640655 | snp | A/G | 6.54001e-05 | 0.00571802 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164122 | ACGCCACAAGGATGT[A/G]CCGGCCCCGGCTGCA | 102465519 |
rs768829841 | snp | C/T | 1.70895e-05 | 0.00292309 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163063 | TGCCATCTGGGGGGG[C/T]GATCTTCATGGGGTA | 102465519 |
rs768954315 | snp | A/G | 1.89961e-05 | 0.00308183 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162987 | GCAGCCCCAGTTCCA[A/G]ACAGAGAAAGGCTAG | 102465519 |
rs769405915 | snp | A/G | 6.69893e-05 | 0.00578707 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164243 | GGAGGCGATCTCAGC[A/G]CACAGGGCCTCCAGC | 102465519 |
rs769528882 | snp | A/G | 2.67799e-05 | 0.00365913 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164126 | CACAAGGATGTGCCG[A/G]CCCCGGCTGCACAGC | 102465519 |
rs769593423 | in-del | -/CT | 5.11252e-05 | 0.00505569 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164088 | AGCCCCTGCCAGCCC[-/CT]GACACGCGCACACAC | 102465519 |
rs769911489 | snp | A/T | 1.65888e-05 | 0.00287996 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163103 | ATGGGCAGTGTCGGG[A/T]CCCCCATCTTTGCAG | 102465519 |
rs770007127 | snp | A/T | 1.65666e-05 | 0.00287802 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163192 | CCTCCTGGGTGAACA[A/T]CTCCAGGGCCCCCCA | 102465519 |
rs770609716 | snp | A/G | 1.65792e-05 | 0.00287912 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163211 | CAGGGCCCCCCAGAA[A/G]AACTCGATGTGCTGG | 102465519 |
rs770712715 | snp | C/G | 1.68397e-05 | 0.00290165 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164261 | CAGGGCCTCCAGCTC[C/G]GTCTCATCATTGATC | 102465519 |
rs771243748 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164499 | CCAGGCCTCTTCCCA[C/T]GTCTGTTTGGAGGCA | 102465519 |
rs771253864 | snp | C/T | 4.23846e-05 | 0.00460331 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163517 | CTCACCACCTCCCCG[C/T]CCAGCCTGGCCCTGG | 102465519 |
rs771827069 | snp | C/T | 0.000378716 | 0.0137555 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164110 | GCGCACACACTCACG[C/T]CACAAGGATGTGCCG | 102465519 |
rs772519068 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164524 | GAGGCAGCGATCCTC[C/T]CTCACTGGCATGGAC | 102465519 |
rs772525644 | snp | C/T | 1.92165e-05 | 0.00309966 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162963 | TGTTCTCCCTTCACA[C/T]GGGGCCTGGCAGCCC | 102465519 |
rs772577788 | snp | C/T | 1.73736e-05 | 0.00294729 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163053 | GTACCTGCTGTGCCA[C/T]CTGGGGGGGCGATCT | 102465519 |
rs772915108 | snp | A/G | 6.70803e-05 | 0.005791 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164249 | GATCTCAGCGCACAG[A/G]GCCTCCAGCTCGGTC | 102465519 |
rs772945401 | in-del | -/AC | 0.00101146 | 0.0224657 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164091 | CCCTGCCAGCCCCTG[-/AC]ACGCGCACACACTCA | 102465519 |
rs773332978 | snp | A/T | | | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162986 | GGCAGCCCCAGTTCC[A/T]AACAGAGAAAGGCTA | 102465519 |
rs773337237 | snp | A/G | 1.65707e-05 | 0.00287838 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163200 | GTGAACATCTCCAGG[A/G]CCCCCCAGAAGAACT | 102465519 |
rs774483717 | snp | A/G | | | synonymous-codon, nc-transcript-variant | HECTD4, MIR6861 | GRCh38.p7 | 12:112163259 | CACTTGGTACATGGT[A/G]TGGGCCTGGGGAGGA | 102465519 |
rs774893697 | in-del | -/G | 1.73791e-05 | 0.00294775 | frameshift-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163055 | CCTGCTGTGCCATCT[-/G]GGGGGGGCGATCTTC | 102465519 |
rs774925570 | snp | C/T | 1.68168e-05 | 0.00289967 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163247 | CTCCATCAGCCCCAC[C/T]TGGTACATGGTGTGG | 102465519 |
rs775441229 | snp | C/T | 0.000224744 | 0.0105982 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163588 | CCGCAGGTGCGCAGC[C/T]CCATCTCCAGTGGGC | 102465519 |
rs775578254 | snp | A/G | 1.92081e-05 | 0.00309898 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162967 | CTCCCTTCACATGGG[A/G]CCTGGCAGCCCCAGT | 102465519 |
rs775660969 | snp | G/T | 1.69092e-05 | 0.00290763 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164273 | CTCGGTCTCATCATT[G/T]ATCTGGAGGGTGGAG | 102465519 |
rs775792386 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163515 | GGCTCACCACCTCCC[C/T]GCCCAGCCTGGCCCT | 102465519 |
rs776958855 | snp | A/G | 1.89813e-05 | 0.00308063 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112162988 | CAGCCCCAGTTCCAA[A/G]CAGAGAAAGGCTAGT | 102465519 |
rs777711984 | snp | A/C | 3.67161e-05 | 0.00428447 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164071 | GGCTGGCTGGCCGGG[A/C]CAGCCCCTGCCAGCC | 102465519 |
rs777958665 | snp | C/G | 4.08622e-05 | 0.00451989 | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163324 | TACCCAGTGCCTCCC[C/G]AGCCCTGGGGTCTGC | 102465519 |
rs778607601 | in-del | -/TCTT | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165217 | CCACCGCGCCTGTCC[-/TCTT]TCTTTTTTTTTTTTT | 102465519 |
rs778932438 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164509 | TCCCACGTCTGTTTG[C/G]AGGCAGCGATCCTCT | 102465519 |
rs779008458 | snp | A/G | 1.67702e-05 | 0.00289566 | missense, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164206 | TGTTGGGGCTGTCAG[A/G]GCTCTCCGTGGCCAG | 102465519 |
rs779335157 | snp | C/T | 3.60334e-05 | 0.00424446 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163036 | ATGGCCAGGGGAGGG[C/T]GGTACCTGCTGTGCC | 102465519 |
rs779368768 | in-del | -/AGAAAA | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112163924 | GTTTTCTTAGTAAAC[-/AGAAAA]CCCTTCTGCTGAGGA | 102465519 |
rs779644404 | snp | A/G | 1.67346e-05 | 0.00289258 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164231 | GGCCAGGTGCTGGGA[A/G]GCGATCTCAGCGCAC | 102465519 |
rs779877711 | snp | A/G | 3.47409e-05 | 0.00416764 | synonymous-codon, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112164120 | TCACGCCACAAGGAT[A/G]TGCCGGCCCCGGCTG | 102465519 |
rs780451477 | snp | C/G | 1.73549e-05 | 0.0029457 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163056 | CCTGCTGTGCCATCT[C/G]GGGGGGCGATCTTCA | 102465519 |
rs780513150 | snp | A/G | 1.65655e-05 | 0.00287793 | synonymous-codon, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163174 | TGATGAACTTGCACA[A/G]CTCCTCCTGGGTGAA | 102465519 |
rs780721981 | snp | A/G | 1.83727e-05 | 0.00303085 | intron-variant, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163024 | CCTACTTGGGACATG[A/G]CCAGGGGAGGGCGGT | 102465519 |
rs781352011 | snp | C/G | 1.6566e-05 | 0.00287797 | missense, downstream-variant-500B | HECTD4, MIR6861 | GRCh38.p7 | 12:112163187 | CAGCTCCTCCTGGGT[C/G]AACATCTCCAGGGCC | 102465519 |
rs796122200 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD4, MIR6861 | GRCh38.p7 | 12:112165161 | CCTGACCTCGTGATC[C/T]ACCCGCCTCAGCCTC | 102465519 |